Organoclay materials for environmentally sensitive regions

ABSTRACT

Fluids comprising oil; and an organophilic clay comprising a smectite clay modified by reaction with a protonated amphoteric surfactant. The smectite clay may be montmorillonite, beidellite, nontronite, or a combination thereof. The protonated amphoteric surfactant may be cetyl/myristyl amine oxide, a stearyl amine oxide, a stearyl betaine, or a combination thereof. In some cases, the fluid may also include water and/or a solid reactive metal.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. patent application Ser. No.11/325,664, filed on Jan. 4, 2006, entitled “Organophilic Clays andMethods for the Preparation Thereof,” and published as US 2007/0155982.

The present invention is related to U.S. patent application Ser. No.11/325,675, entitled “Organophilic Clays and Methods for the Preparationand Use Thereof,” filed on the same date herewith, the entire disclosureof which is incorporated herein by reference.

BACKGROUND

The present invention relates to organophilic clays. More particularly,the present invention relates to organophilic clays that comprise asmectite clay modified by reaction with a protonated amphotericsurfactant, and methods for the preparation and use thereof.

Organophilic clays may be used in a wide variety of subterraneanapplications. As used herein, the term “organophilic clay” refers to aclay that is compatible with oils. In subterranean applications,organophilic clays are widely used, for example, in various cementingand sealing operations as well as to add viscosity and/or suspendingpower to various fluids. In addition to subterranean applications,organophilic clays also may be used in a variety of surfaceapplications, for example, as a viscosifying agents, suspending agents,and the like.

In some instances, organophilic clays may comprise a smectite clay thathas been modified by a cation exchange reaction with a fatty quaternaryammonium surfactant. Generally, the quaternary ammonium surfactantimparts some organophilic character to the clay. However, this class ofchemicals has proved challenging from an environmental standpoint. Forinstance, the quaternary ammonium surfactants used heretofore may haveundesirable environmental characteristics and/or may be limited bystrict environmental regulations in certain areas of the world. As aresult, use of these quaternary ammonium surfactants in subterraneanapplications may result in the potential for the bioaccumulation and/orpersistence of the quaternary ammonium surfactants in the environment,which may create potential dangers for the use of the quaternaryammonium surfactants, such as adverse effects on shrimp and otheraqueous aquatic species. Accordingly, in more environmentally sensitiveregions, such as the North Sea, quaternary ammonium surfactantsgenerally are not acceptable, and therefore the use of organophilicclays produced using quaternary surfactants is also not acceptable.

SUMMARY

The present invention relates to organophilic clays. More particularly,the present invention relates to organophilic clays that comprise asmectite clay modified by reaction with a protonated amphotericsurfactant, and methods for the preparation and use thereof.

In one embodiment, the present invention provides an organophilic claycomprising a smectite clay modified by reaction with a protonatedamphoteric surfactant.

Another embodiment of the present invention provides a fluid comprisingan oil and an organophilic clay comprising a smectite clay modified byreaction with a protonated amphoteric surfactant.

Another embodiment of the present invention provides a drilling fluidcomprising an oil, water, and an organophilic clay comprising a smectiteclay modified by reaction with a protonated amphoteric surfactant.

The features and advantages of the present invention will be apparent tothose skilled in the art. While numerous changes may be made by thoseskilled in the art, such changes are within the spirit of the invention.

DESCRIPTION OF PREFERRED EMBODIMENTS

The present invention relates to organophilic clays. More particularly,the present invention relates to organophilic clays that comprise asmectite clay modified by reaction with a protonated amphotericsurfactant, and methods for the preparation and use thereof.

The organophilic clays of the present invention comprise a smectite claymodified by reaction with a protonated amphoteric surfactant. Amongother things, the organophilic clays of the present invention may beused in subterranean and surface applications as viscosifying agentsand/or suspending agents. For example, the organophilic clays of thepresent invention may be used as viscosifying agents in cementing,sealing, and/or drilling operations.

A wide variety of smectite clays may be used in the present invention.Generally, smectite clays contain exchangeable cations, such as sodium,potassium, calcium, barium, and the like. These exchangeable cationsallow for reaction with the protonated amphoteric surfactant through acation exchange reaction to form the organophilic clays of the presentinvention. Suitable smectite clays, include, but are not limited to,montmorillonite, beidellite, nontronite, and combinations thereof.Montmorillonite is commonly referred to as “bentonite.”

The organophilic clays of the present invention further comprise aprotonated amphoteric surfactant. The protonated amphoteric surfactantsshould adsorb onto the smectite clay through a cation exchange reactionto form the organophilic clays of the present invention. In someembodiments, the protonated amphoteric surfactant may be substituted foran amount in the range of from about 25% to about 100% of theexchangeable cations of the smectite clay. In some embodiments, theprotonated amphoteric surfactant may be substituted for an amount in therange of from about 40% to about 70% of the exchangeable cations of thesmectite clay. The degree of substitution depends on a number of factorssuch as the processing technique used to prepare the organophilic clay,the temperature of the processing technique, and the particularexchangeable cations of the smectite clay.

Suitable amphoteric surfactants include, but are not limited to, amineoxides, betaines, phosphobetaines, imidazolines, sultaines, andcombinations thereof. Example of a suitable amine oxides arecetyl/myristyl amine oxide and stearyl amine oxide. An example of asuitable betaine is stearyl betaine. While the alkyl chain length of theamphoteric surfactants may vary, in some embodiments, the amphotericsurfactants may have an alkyl chain length in the range of from about 12carbon atoms to about 24 carbon atoms. Those of ordinary skill in theart, with the benefit of this disclosure, will be able to select asuitable amphoteric surfactant and carbon chain length based on a numberof factors, including, but not limited to, cost, environmental concerns,and the particular application.

The amphoteric surfactants may be protonated using any suitableprocessing technique. In some embodiments, the amphoteric surfactantsmay be protonated by lowering the pH thereof, for example, by mixing anamphoteric surfactant with an acid. The pH of the amphoteric surfactantshould be lowered in an amount sufficient to provide the desired degreeof protonation. In some embodiments, the amphoteric surfactant may becompletely protonated. Where an acid is used to lower the pH of theamphoteric surfactant, the acid should have a pH below the pKa value ofthe surfactant. As used herein, the “pKa value” refers to the negativelog of the ionization constant (“Ka”). Any of a variety of acids may besuitable to lower the pH of the amphoteric surfactant, including, butnot limited, to organic and mineral acids. For example, hydrochloricacid and acetic acid may be suitable.

The organophilic clays of the present invention may be prepared usingany suitable processing technique. Generally, preparation of anorganophilic clay of the present invention comprises reacting a smectiteclay and a protonated amphoteric surfactant. In one embodiment, reactingthe smectite clay and the protonated amphoteric surfactant comprisesapplying a protonated amphoteric surfactant to a dry smectite clay, forexample, during extrusion or grinding of the dry smectite clay. Inanother embodiment, reacting the smectite clay and the protonatedamphoteric surfactant comprises mixing a protonated amphotericsurfactant with a mixture of water and a smectite clay. The waterincluded in this mixture may be freshwater, saltwater (e.g., watercontaining one or more salts dissolved therein), brine (e.g., saturatedsaltwater produced from subterranean formations), or seawater, orcombinations thereof. Flocculation and filtration in water are twoindicators of organophilic modification. For example, flocculation ofthe smectite clay out of the water after mixture therewith indicatesorganophilic modification. Filtration may provide a physical indicationof organophilic modifications in that organophilic clays are hydrophobicso should agglomerate allowing the filtration off of the water, whereasan unmodified clay will not agglomerate and should plug the filter.

As previously discussed the organophilic clays of the present inventionmay be suitable for use in a variety of subterranean and surfaceapplications. In some embodiments, the organophilic clays may beincluded in a fluid that comprises an oil and an organophilic clay ofthe present invention that comprises a smectite clay modified byreaction with a protonated amphoteric surfactant. Among other things,the organophilic clay may be included in the fluid as a viscosifyingagent and/or a suspending agent. In some embodiments, the fluid may bean oil suspension that further comprises a solid additive suspended inthe oil. In some embodiments, the fluid may be an emulsion (e.g.,oil-in-water or water-in-oil), wherein the organophilic clay is presentin the oil phase of the emulsion and/or at the interface of the oil andwater phase. In some embodiments, the organophilic clay may act tostabilize the emulsion. In some embodiments, the fluid may be an invertemulsion drilling fluid. In some embodiments, the fluid may be asubterranean treatment fluid, such as a drilling fluid.

Suitable oils that may be included in the fluids of the presentinvention, include, but are not limited to, diesel oils, paraffinicoils, olefinic oils, mineral oils, vegetable oils, long chain esters,and combinations thereof. Where used, for example, in an emulsion, thewater that may be included in the fluids of the present invention mayinclude freshwater, saltwater (e.g., water containing one or more saltsdissolved therein), brine (e.g., saturated saltwater produced fromsubterranean formations), or seawater, or combinations thereof.

Additionally, in some embodiments, the fluids of the present inventionfurther may comprise a solid additive suspended in the oil. Examples ofsuitable solid additives include, but are not limited to, polymers,reactive metals, and combinations thereof. Inclusion of these solidadditives in these oil suspensions, among other things, may facilitatethe transport of the solid additive and/or mixing of the solid additivewith water. In some embodiments, the oil suspensions further may becombined with water and then introduced into a well bore that penetratesa subterranean formation. The water that may be combined with the oilsuspension may include freshwater, saltwater (e.g., water containing oneor more salts dissolved therein), brine (e.g., saturated saltwaterproduced from subterranean formations), or seawater, or combinationsthereof.

Depending on the particular application, additional additives may beincluded in the fluids of the present invention as desired by one ofordinary skill in the art. Suitable additives include, but are notlimited to, dispersants, emulsifiers, salts, weighting agents,defoamers, and a variety of other suitable additives. For example,mono-, di-, and/or trivalent salts may be included in the fluids of thepresent invention, for example, to mitigate the swelling of formationclays.

An example method of the present invention comprises providing a fluidcomprising an organophilic clay, the organophilic clay comprising asmectite clay modified by reaction with a protonated amphotericsurfactant; and introducing the fluid into a well bore that penetrates asubterranean formation. In some embodiments, the methods of the presentinvention further may comprise combining the fluid with water prior tothe step of introducing the fluid into a well bore, for example, wherethe fluid is an oil suspension that further comprises a solid additivesuspended in the oil.

Another example method of the present invention is a method of drillinga well bore, the method comprising providing a drilling fluid comprisingan oil and an organophilic clay, the organophilic clay comprising asmectite clay modified by reaction with a protonated amphotericsurfactant; introducing the drilling fluid into the well bore; anddrilling the well bore. Any suitable technique for drilling the wellbore may be used in accordance with the methods of the presentinvention. As previously mentioned, in some embodiments, the drillingfluid may be an emulsion that comprising an oil phase and a water phase,wherein the organophilic clay is present in the oil phase. In someembodiments, the drilling fluid may be an invert emulsion.

To facilitate a better understanding of the present invention, thefollowing example(s) of certain aspects of some embodiments are given.In no way should the following example(s) be read to limit, or define,the scope of the invention.

EXAMPLE

An organophilic clay was prepared using the following procedure. First,a cetyl/myristyl amine oxide having a yellow rating for Norway as of2005 was treated with hydrochloric acid to reduce the pH to about 3, atwhich point the cetyl/myristyl amine oxide was protonated. Additionally,water and bentonite clay in an amount of 5% by weight of the mixture wasplaced in a Waring® blender and sheared for about 15 minutes to ensuresubstantially full hydration of the clay. Then, the protonatedcetyl/myristyl amine oxide was added slowly to this mixture, and theslurry gained viscosity rapidly. The addition of the protonatedcetyl/myristyl amine oxide surfactant was stopped when the viscosity ofthe slurry decreased and became low due to flocculation of the clay outof the water, indicating organophilic modification. Thereafter, theflocculated clay was filtered and dried in a vacuum oven overnight,after which the filtered and dried organophilic clay was ground into apowder.

Once prepared, the powder ground from the filtered and dried clay wasadded to a 70/30 mixture of a long chain mineral oil (ESCAID™ 110 oilfrom Exxon, Houston, Tex.) and water, and stirred for about 30 minutes.The result was an almost completely homogeneous thickening of themixture by the clay. The mixture had only a slight amount of top oil andan emulsion stability reading of about 120 volts after standing forabout 2 hours and showed no significant signs of settling overnight. Theemulsion stability was determined using a FANN® ES Tester, from FannInstrument Company, Houston, Tex.

Therefore, the present invention is well adapted to attain the ends andadvantages mentioned as well as those that are inherent therein. Theparticular embodiments disclosed above are illustrative only, as thepresent invention may be modified and practiced in different butequivalent manners apparent to those skilled in the art having thebenefit of the teachings herein. Furthermore, no limitations areintended to the details of construction or design herein shown, otherthan as described in the claims below. It is therefore evident that theparticular illustrative embodiments disclosed above may be altered ormodified and all such variations are considered within the scope andspirit of the present invention. In particular, every range of values(of the form, “from about a to about b,” or, equivalently, “fromapproximately a to b,” or, equivalently, “from approximately a-b”)disclosed herein is to be understood as referring to the power set (theset of all subsets) of the respective range of values, and set forthevery range encompassed within the broader range of values. Also, theterms in the claims have their plain, ordinary meaning unless otherwiseexplicitly and clearly defined by the patentee. Therefore, the presentinvention is well adapted to attain the ends and advantages mentioned aswell as those that are inherent therein. While numerous changes may bemade by those skilled in the art, such changes are encompassed withinthe spirit of this present invention as defined by the appended claims.

What is claimed is:
 1. A fluid comprising an oil; and an organophilicclay comprising a protonated amphoteric surfactant modified smectiteclay, and the protonated amphoteric surfactant is substituted for anamount in the range of from about 25% to about 100% of the exchangeablecations, and, the protonated amphoteric surfactant comprises aphosphobetaine, an imidazoline, a cetyl/myristyl amine oxide, a stearylamine oxide, a stearyl betaine, and combinations thereof.
 2. The fluidof claim 1 wherein the fluid is an emulsion.
 3. The fluid of claim 1wherein the oil is selected from the group consisting of a diesel oil, aparaffinic oil, an olefinic oil, a mineral oil, a vegetable oil, a longchain ester, and combinations thereof.
 4. The fluid of claim 1 whereinthe smectite clay is selected from the group consisting ofmontmorillonite, beidellite, nontronite, and combinations thereof. 5.The fluid of claim 1 wherein the protonated amphoteric surfactant has analkyl chain length of from about 12 carbon atoms to about 24 carbonatoms.
 6. The fluid of claim 1 wherein the smectite clay comprisesmontmorillonite and the protonated amphoteric surfactant comprises anamine oxide.
 7. The fluid of claim 1 wherein the fluid further comprisesa solid additive suspended in the oil, the solid additive selected fromthe group consisting of a polymer, a reactive metal, and combinationsthereof.
 8. A fluid comprising an oil; water; and an organophilic claycomprising a protonated amphoteric surfactant modified smectite clay,and the protonated amphoteric surfactant is substituted for an amount inthe range of from about 25% to about 100% of the exchangeable cations,the protonated amphoteric surfactant comprises a phosphobetaine, animidazoline, a cetyl/myristyl amine oxide, a stearyl amine oxide, astearyl betaine, and combinations thereof wherein the fluid is suitablefor use as a drilling fluid.
 9. The fluid of claim 8 wherein the fluidis an invert emulsion.
 10. The fluid of claim 8 wherein the oil isselected from the group consisting of a diesel oil, a paraffinic oil, anolefinic oil, a mineral oil, a vegetable oil, a long chain ester, andcombinations thereof.
 11. The fluid of claim 8 wherein the smectite clayis selected from the group consisting of montmorillonite, beidellite,nontronite, and combinations thereof.
 12. The fluid of claim 8 whereinthe protonated amphoteric surfactant has an alkyl chain length of fromabout 12 carbon atoms to about 24 carbon atoms.
 13. The fluid of claim 8wherein the smectite clay comprises montmorillonite and the protonatedamphoteric surfactant comprises an amine oxide.
 14. The fluid of claim 8wherein the fluid further comprises a solid additive suspended in theoil, the solid additive selected from the group consisting of a polymer,a reactive metal, and combinations thereof.
 15. A fluid comprising:water; a solid reactive metal; an oil selected from the group consistingof a diesel oil, a paraffinic oil, an olefinic oil, a mineral oil, avegetable oil, a long chain ester, and combinations thereof; and,cetyl/myristyl amine oxide modified montmorillonite; wherein the fluidis an invert emulsion suitable for use as a drilling fluid.